Canonical Allele Identifier: CA2679047123

Gene: MMUT

Linked Data

• gnomAD v4: 6-49458158-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49458159_49458160del , CM000668.2:g.49458159_49458160del	GRCh38
NC_000006.11:g.49425872_49425873del , CM000668.1:g.49425872_49425873del	GRCh37
NC_000006.10:g.49533831_49533832del	NCBI36
NG_007100.1:g.9980_9981del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.386-102_386-101del MANE Select	ENSP00000274813.3:n.386-102_386-101del
ENST00000274813.3:c.386-102_386-101del	ENSP00000274813.3:n.386-102_386-101del
NM_000255.3:c.386-102_386-101del	NP_000246.2:n.386-102_386-101del
XM_005249143.2:c.386-102_386-101del	XP_005249200.1:n.386-102_386-101del
XM_005249143.3:c.386-102_386-101del	XP_005249200.1:n.386-102_386-101del
NM_000255.4:c.386-102_386-101del MANE Select	NP_000246.2:n.386-102_386-101del